2-Amino-5-bromo-3-picoline

Names

[ Name ]:
2-Amino-5-bromo-3-picoline

[Synonym ]:
2-Amina-5-bromo-3-picoline
5-bromo-3-methylpyridin-2-amine
2-AMINO-3-METHYL-5-BROMOPYRIDINE
2-Amino-5-bromo-3-methyl
MFCD00068232
2-Pyridinamine, 5-bromo-3-methyl-
2-Amino-5-bromo-3-picoline
2-PyridinaMine,5-broMo-3-Methyl
5-bromo-3-methylpyridin-2-ylamine
2-amino-5-bromo-3-methyl pyridine
6-amino-3-bromo-5-methylpyridine
5-bromo-3-methyl-2-aminopyridine

Biological Activity

[Description]:

5-Bromo-3-methylpyridin-2-amine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
250.0±35.0 °C at 760 mmHg

[ Melting Point ]:
88-95 °C(lit.)

[ Molecular Formula ]:
C₆H₇BrN₂

[ Molecular Weight ]:
187.04

[ Flash Point ]:
105.0±25.9 °C

[ Exact Mass ]:
185.979248

[ PSA ]:
38.91000

[ LogP ]:
2.44

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.617

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

2, 5-and 5, 6-Dihalonicotinic acids and their precursors. Setliff FL.

J. Chem. Eng. Data 15(4) , 590-591, (1970)

Ring contraction of 2-azidopyridine 1-oxides and related compounds. 2-Cyano-1-hydroxypyrroles and-imidazoles. Abramovitch RA and Cue Jr BW.

J. Am. Chem. Soc. 98(6) , 1478-1486, (1976)

Synthesis of the grass alkaloid perlolidine through a pyridyne cyclisation reaction. Kessar SV and Singh P.

Indian J. Chem. B 40(11) , 1129-1131, (2001)

Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.